Canonical Allele Identifier: CA367873476

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81340829C>A (hg19) ; chr7:g.81711513C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81711513C>A , CM000669.2:g.81711513C>A	GRCh38
NC_000007.13:g.81340829C>A , CM000669.1:g.81340829C>A	GRCh37
NC_000007.12:g.81178765C>A	NCBI36
NG_016274.1:g.63624G>T
NG_016274.2:g.63624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1412G>T MANE Select	ENSP00000222390.5:p.Gly471Val
ENST00000457544.7:c.1397G>T	ENSP00000391238.2:p.Gly466Val
ENST00000222390.9:c.1412G>T	ENSP00000222390.5:p.Gly471Val
ENST00000457544.6:c.1397G>T	ENSP00000391238.2:p.Gly466Val
NM_000601.4:c.1412G>T	NP_000592.3:p.Gly471Val
NM_001010932.1:c.1397G>T	NP_001010932.1:p.Gly466Val
XM_006715956.2:c.1412G>T	XP_006716019.1:p.Gly471Val
XM_011516115.1:c.1397G>T	XP_011514417.1:p.Gly466Val
NM_000601.5:c.1412G>T	NP_000592.3:p.Gly471Val
NM_001010932.2:c.1397G>T	NP_001010932.1:p.Gly466Val
XM_011516115.2:c.1397G>T	XP_011514417.1:p.Gly466Val
NM_000601.6:c.1412G>T MANE Select	NP_000592.3:p.Gly471Val
NM_001010932.3:c.1397G>T	NP_001010932.1:p.Gly466Val